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Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature

Identifieur interne : 000473 ( PascalFrancis/Corpus ); précédent : 000472; suivant : 000474

Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature

Auteurs : S. R. Hoque ; S. Mansour ; P. S. Mortimer

Source :

RBID : Pascal:07-0273501

Descripteurs français

English descriptors

Abstract

Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
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A02 01      @0 BJDEAZ
A03   1    @0 Br. j. dermatol. : (1951)
A05       @2 156
A06       @2 6
A08 01  1  ENG  @1 Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature
A11 01  1    @1 HOQUE (S. R.)
A11 02  1    @1 MANSOUR (S.)
A11 03  1    @1 MORTIMER (P. S.)
A14 01      @1 Department of Dermatology, St Helier Hospital @2 Carshalton, Surrey SM5 1AA @3 GBR @Z 1 aut.
A14 02      @1 SW Thames Regional Genetics Unit, St George's Hospital, University of London @2 London SW17 0RE @3 GBR @Z 2 aut.
A14 03      @1 Dermatology Unit, Cardiac and Vascular Sciences, St George's Hospital, University of London @2 London SW17 0RE @3 GBR @Z 3 aut.
A20       @1 1230-1234
A21       @1 2007
A23 01      @0 ENG
A43 01      @1 INIST @2 1043 @5 354000149620140120
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 24 ref.
A47 01  1    @0 07-0273501
A60       @1 P
A61       @0 A
A64 01  1    @0 British journal of dermatology : (1951)
A66 01      @0 GBR
C01 01    ENG  @0 Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.
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C02 02  X    @0 002B12B04
C03 01  X  FRE  @0 Ongle jaune syndrome @5 01
C03 01  X  ENG  @0 Yellow nail syndrome @5 01
C03 01  X  SPA  @0 Uña amarilla síndrome @5 01
C03 02  X  FRE  @0 Lymphoedème @5 02
C03 02  X  ENG  @0 Lymphedema @5 02
C03 02  X  SPA  @0 Linfedema @5 02
C03 03  X  FRE  @0 Génétique @5 09
C03 03  X  ENG  @0 Genetics @5 09
C03 03  X  SPA  @0 Genética @5 09
C03 04  X  FRE  @0 Désordre @5 10
C03 04  X  ENG  @0 Disorder @5 10
C03 04  X  SPA  @0 Desorden @5 10
C03 05  X  FRE  @0 Article synthèse @5 11
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C03 05  X  SPA  @0 Artículo síntesis @5 11
C03 06  X  FRE  @0 Dermatologie @5 12
C03 06  X  ENG  @0 Dermatology @5 12
C03 06  X  SPA  @0 Dermatología @5 12
C07 01  X  FRE  @0 Peau pathologie @5 37
C07 01  X  ENG  @0 Skin disease @5 37
C07 01  X  SPA  @0 Piel patología @5 37
C07 02  X  FRE  @0 Appareil circulatoire pathologie @5 38
C07 02  X  ENG  @0 Cardiovascular disease @5 38
C07 02  X  SPA  @0 Aparato circulatorio patología @5 38
C07 03  X  FRE  @0 Lymphatique pathologie @5 39
C07 03  X  ENG  @0 Lymphatic vessel disease @5 39
C07 03  X  SPA  @0 Linfático patología @5 39
N21       @1 183
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 07-0273501 INIST
ET : Yellow nail syndrome : not a genetic disorder? Eleven new cases and a review of the literature
AU : HOQUE (S. R.); MANSOUR (S.); MORTIMER (P. S.)
AF : Department of Dermatology, St Helier Hospital/Carshalton, Surrey SM5 1AA/Royaume-Uni (1 aut.); SW Thames Regional Genetics Unit, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (2 aut.); Dermatology Unit, Cardiac and Vascular Sciences, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (3 aut.)
DT : Publication en série; Niveau analytique
SO : British journal of dermatology : (1951); ISSN 0007-0963; Coden BJDEAZ; Royaume-Uni; Da. 2007; Vol. 156; No. 6; Pp. 1230-1234; Bibl. 24 ref.
LA : Anglais
EA : Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.
CC : 002B08H; 002B12B04
FD : Ongle jaune syndrome; Lymphoedème; Génétique; Désordre; Article synthèse; Dermatologie
FG : Peau pathologie; Appareil circulatoire pathologie; Lymphatique pathologie
ED : Yellow nail syndrome; Lymphedema; Genetics; Disorder; Review; Dermatology
EG : Skin disease; Cardiovascular disease; Lymphatic vessel disease
SD : Uña amarilla síndrome; Linfedema; Genética; Desorden; Artículo síntesis; Dermatología
LO : INIST-1043.354000149620140120
ID : 07-0273501

Links to Exploration step

Pascal:07-0273501

Le document en format XML

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<div type="abstract" xml:lang="en">Background Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS. Objectives To conduct a retrospective survey investigating the genetic basis of YNS. Methods The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients. Results Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes. Conclusions This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.</div>
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<AU>HOQUE (S. R.); MANSOUR (S.); MORTIMER (P. S.)</AU>
<AF>Department of Dermatology, St Helier Hospital/Carshalton, Surrey SM5 1AA/Royaume-Uni (1 aut.); SW Thames Regional Genetics Unit, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (2 aut.); Dermatology Unit, Cardiac and Vascular Sciences, St George's Hospital, University of London/London SW17 0RE/Royaume-Uni (3 aut.)</AF>
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